HuGE Literature Finder
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| Analysis of AVPR1A, thermal and pressure pain thresholds, and stress in sickle cell disease. Frontiers in pain research (Lausanne, Switzerland) 2023 1 3 1060245. Powell-Roach Keesha L, Yao Yingwei, Cao Xueyuan, Chamala Srikar, Wallace Margaret R, Cruz-Almeida Yenisel, Molokie Robert E, Wang Zaijie Jim, Wilkie Diana |
| Association between The SIRT1 and SIRT3 Levels and Gene Polymorphisms with Infertility in War Zones of Kermanshah Province, Iran: A Case-Control Study. International journal of fertility & sterility 2023 3 17 (2): 120-126. Nasiri Abolfazl, Hosseini Sayed Mostafa, Rashidi Mohsen, Mozafari Ha |
| Impact of Superoxide Dismutase Genetic Polymorphism (SOD2 Val16Ala) and Superoxide Dismutase Level on Disease Severity in a Cohort of Egyptian Sickle Cell Disease Patients. Mediterranean journal of hematology and infectious diseases 2022 14 (1): e2022037. Khorshied Mervat M, Shaheen Iman A, Selim Yasmeen M M, Elshahawy Asmaa O, Youssry Ilh |
| Influence of Haptoglobin Polymorphism on Stroke in Sickle Cell Disease Patients. Genes 2022 1 13 (1): . Edwards Olivia, Burris Alicia, Lua Josh, Wilkie Diana J, Ezenwa Miriam O, Doré Sylva |
| The protective effect of the spleen in sickle cell patients. A comparative study between patients with asplenia/hyposplenism and hypersplenism. Frontiers in physiology 2022 9 13 796837. Peretz Sari, Livshits Leonid, Pretorius Etheresia, Makhro Asya, Bogdanova Anna, Gassmann Max, Koren Ariel, Levin Cari |
| Oxidative stress, inflammation, blood rheology, and microcirculation in adults with sickle cell disease: Effects of hydroxyurea treatment and impact of sickle cell syndrome. European journal of haematology 2021 2 106 (6): 800-807. Connes Philippe, Möckesch Berenike, Tudor Ngo Sock Emilienne, Hardy-Dessources Marie-Dominique, Reminy Karen, Skinner Sarah, Billaud Marie, Nader Elie, Tressieres Benoit, Etienne-Julan Maryse, Guillot Nicolas, Lemonne Nathalie, Hue Olivier, Romana Marc, Antoine-Jonville Soph |
| Influence of rs1042713 and rs1042714 polymorphisms of ?2-adrenergic receptor gene with erythrocyte cAMP in sickle cell disease patients from Odisha State, India. Annals of hematology 2020 Sep . Sinha Shalini, Jit Bimal Prasad, Patro A Raj Kumar, Ray Aisurya, Dehury Snehadhini, Sahoo Sarmila, Behera Rajendra Kumar, Mohanty Pradeep Kumar, Panigrahi Pinaki, Das Padmala |
| GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death. EBioMedicine 2020 Jul 57 102843. Juang Jyh-Ming Jimmy, Binda Anna, Lee Shyh-Jye, Hwang Juey-Jen, Chen Wen-Jone, Liu Yen-Bin, Lin Lian-Yu, Yu Chih-Chieh, Ho Li-Ting, Huang Hui-Chun, Chen Ching-Yu Julius, Lu Tzu-Pin, Lai Liang-Chuan, Yeh Shih-Fan Sherri, Lai Ling-Ping, Chuang Eric Y, Rivolta Ilaria, Antzelevitch Charl |
| Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation. PloS one 2020 12 15 (12): e0243649. Koponen Mikael, Marjamaa Annukka, Tuiskula Annukka M, Viitasalo Matti, Nallinmaa-Luoto Terhi, Leinonen Jaakko T, Widen Elisabeth, Toivonen Lauri, Kontula Kimmo, Swan Heik |
| The CYB5R3 and G6PD A alleles modify severity of anemia in malaria and sickle cell disease. American journal of hematology 2020 7 95 (11): 1269-1279. Gordeuk Victor R, Shah Binal N, Zhang Xu, Thuma Philip E, Zulu Stenford, Moono Rodgers, Reading N Scott, Song Jihyun, Zhang Yingze, Nouraie Mehdi, Campbell Andrew, Minniti Caterina P, Rana Sohail R, Darbari Deepika S, Kato Gregory J, Niu Mei, Castro Oswaldo L, Machado Roberto, Gladwin Mark T, Prchal Josef |
| Influence of ?-Globin Haplotypes on Oxidative Stress, Antioxidant Capacity and Inflammation in Sickle Cell Patients of Chhattisgarh. Indian journal of clinical biochemistry : IJCB 2019 5 34 (2): 201-206. Bhagat Sanjana, Thakur Amar Sin |
| Red blood cell alloimmunization and minor red blood cell antigen phenotypes in transfused Ghanaian patients with sickle cell disease. Transfusion 2019 2 59 (6): 2016-2022. Boateng Lilian A, Campbell Andrew D, Davenport Robertson D, Osei-Akoto Alex, Hugan Sheri, Asamoah Akwasi, Schonewille He |
| Serum Iron Levels and Copper-to-Zinc Ratio in Sickle Cell Disease. Medicina (Kaunas, Lithuania) 2019 5 55 (5): . Antwi-Boasiako Charles, Dankwah Gifty B, Aryee Robert, Hayfron-Benjamin Charles, Doku Alfred, N'guessan Benoit Banga, Asiedu-Gyekye Isaac Julius, Campbell Andrew |
| Vasopressin SNP pain factors and stress in sickle cell disease. PloS one 2019 14 (11): e0224886. Powell-Roach Keesha L, Yao Yingwei, Jhun Ellie H, He Ying, Suarez Marie L, Ezenwa Miriam O, Molokie Robert E, Wang Zaijie Jim, Wilkie Diana |
| GSTT1 (rs4025935) null genotype is associated with increased risk of sickle cell disease in the populations of Tabuk-Northwestern region of Saudi Arabia. Hematology (Amsterdam, Netherlands) 2017 Apr 22 (3): 172-177. Abu-Duhier Faisel, Mir Rash |
| Evaluation of Alpha-1 Antitrypsin Levels and SERPINA1 Gene Polymorphisms in Sickle Cell Disease. Frontiers in immunology 2017 11 8 1491. Carvalho Magda Oliveira Seixas, Souza André Luís Carvalho Santos, Carvalho Mauricio Batista, Pacheco Ana Paula Almeida Souza, Rocha Larissa Carneiro, do Nascimento Valma Maria Lopes, Figueiredo Camylla Vilas Boas, Guarda Caroline Conceição, Santiago Rayra Pereira, Adekile Adekunle, Goncalves Marilda de Sou |
| Relation between glutathione S-transferase genes (GSTM1, GSTT1, and GSTP1) polymorphisms and clinical manifestations of sickle cell disease in Egyptian patients. Hematology (Amsterdam, Netherlands) 2015 Apr . Ellithy Hend N, Yousri Sherif, Shahin Gehan |
| Severity of Brazilian sickle cell disease patients: severity scores and feasibility of the Bayesian network model use. Blood cells, molecules & diseases 2015 Apr 54 (4): 321-7. Belini Junior Edis, Silva Danilo Grünig Humberto, Torres Lidiane de Souza, Okumura Jéssika Viviani, Lobo Clarisse Lopes de Castro, Bonini-Domingos Claudia Regi |
| Alterations of a Cellular Cholesterol Metabolism Network Are a Molecular Feature of Obesity-Related Type 2 Diabetes and Cardiovascular Disease. Diabetes 2015 7 64 (10): 3464-74. Ding Jingzhong, Reynolds Lindsay M, Zeller Tanja, Müller Christian, Lohman Kurt, Nicklas Barbara J, Kritchevsky Stephen B, Huang Zhiqing, de la Fuente Alberto, Soranzo Nicola, Settlage Robert E, Chuang Chia-Chi, Howard Timothy, Xu Ning, Goodarzi Mark O, Chen Y-D Ida, Rotter Jerome I, Siscovick David S, Parks John S, Murphy Susan, Jacobs David R, Post Wendy, Tracy Russell P, Wild Philipp S, Blankenberg Stefan, Hoeschele Ina, Herrington David, McCall Charles E, Liu Yongm |
| Association of DNA Damage Repair Gene Polymorphisms hOGG1, XRCC1and p53 with Sickle Cell Disease Patients in India. Mediterranean journal of hematology and infectious diseases 2015 7 (1): e2015046. Nishank Sudhansu Sekh |
| Genetic variation in healthy oldest-old. PloS one 2009 4 (8): e6641. Halaschek-Wiener Julius, Amirabbasi-Beik Mahsa, Monfared Nasim, Pieczyk Markus, Sailer Christian, Kollar Anita, Thomas Ruth, Agalaridis Georgios, Yamada So, Oliveira Lisa, Collins Jennifer A, Meneilly Graydon, Marra Marco A, Madden Kenneth M, Le Nhu D, Connors Joseph M, Brooks-Wilson Angela |
| Glutathione S-transferase gene polymorphisms (GSTM1, GSTT1, and GSTP1) in Egyptian pediatric patients with sickle cell disease. Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 0 17 (4): 265-70. Shiba Hala Fathy, El-Ghamrawy Mona Kamal, Shaheen Iman Abd El-Mohsen, Ali Rasha Abd El-Ghani, Mousa Somaia Mohamm |
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- Page last updated:Mar 28, 2023
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